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Familial hyperproinsulinaemia due to a mutation substituting histidine for arginine at position 65 in proinsulin: identification of the mutation by restriction enzyme mapping

✍ Scribed by Collinet, M.; Berthelon, M.; Bénit, P.; Laborde, K.; Desbuquois, B.; Munnich, A.; Robert, J. J.


Book ID
113042875
Publisher
Springer
Year
1998
Tongue
English
Weight
313 KB
Volume
157
Category
Article
ISSN
0340-6997

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